607731-83-9

Basic information

• Product Name: 4-phenoxy-2-phenylaniline
• Synonyms: 4-phenoxy-2-phenylaniline
• CAS NO: 607731-83-9
• Molecular Weight: 261.323
• Mol File: 607731-83-9.mol

Chemical Properties

• CAS DataBase Reference: 4-phenoxy-2-phenylaniline(CAS DataBase Reference)
• NIST Chemistry Reference: 4-phenoxy-2-phenylaniline(607731-83-9)
• EPA Substance Registry System: 4-phenoxy-2-phenylaniline(607731-83-9)

Safety Data

• Hazardous Substances Data: 607731-83-9(Hazardous Substances Data)

Upstream product

• 607731-81-7 (2-iodo-4-phenoxy-phenyl)-carbamic acid tert-butyl ester 
• 607731-80-6 tert-butyl (4-phenoxyphenyl)carbamate 
• 139-59-3 4-phenoxyanilin 
• 607731-82-8 2-iodo-4-phenoxyaniline 
• 98-80-6 phenylboronic acid 

Downstream Products

• 63317-69-1 1-phenyldibenzo[b,d]furan 
• 607731-75-9 2-iodo-5-phenoxy-1,1'-biphenyl 

Relevant articles and documents

Synthesis of fused polycycles by 1,4-palladium migration chemistry

Novel palladium migration/arylation methodology for the synthesis of complex fused polycycles has been developed, in which one or more sequential Pd-catalyzed intramolecular migration processes involving C-H activation are employed. The chemistry works best with electron-rich aromatics, which is in agreement with the idea that these palladium-catalyzed C-H activation reactions parallel electrophilic aromatic substitution.

1,4-Palladium migration via C-H activation, followed by arylation: Synthesis of fused polycycles

A novel palladium migration/arylation methodology for the synthesis of complex fused polycycles has been developed, in which one or more sequential Pd-catalyzed intramolecular migration processes involving C-H activation are employed. The chemistry works best with electron-rich aromatics, which is in agreement with the idea that these palladium-catalyzed C-H activation reactions parallel electrophilic aromatic substitution. Copyright